# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/127d8083-0ecc-4699-a8e3-a5a6624f8391

> Inspection records and compliance data for OneBlood, Inc. in Winter Springs, Florida. Access full analysis and detailed observations.

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## Details

- Name: OneBlood, Inc.
- FEI Number: 1036321
- City: Winter Springs
- State: Florida
- Country Name: United States
- Address Line 1: 268 E State Road 434
- Zip Code: 32708

## Related Documents

- [FDA Inspection 1166604 - OneBlood, Inc. - 2022-04-05](https://www.keypedia.com/records/fda_inspections/oneblood-inc/73fb19d8-905f-43a4-bcb7-2299c7a11e07) — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2022
- [FDA Inspection 1166604 - OneBlood, Inc. - 2022-04-05](https://www.keypedia.com/records/fda_inspections/oneblood-inc/920c211f-61d9-46ae-8b04-e2210b89df82) — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2022
- [FDA Inspection 1088447 - OneBlood, Inc. - 2019-04-15](https://www.keypedia.com/records/fda_inspections/oneblood-inc/9a520134-fd98-4818-bc95-348374fcdf92) — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2019
- [FDA Inspection 949254 - OneBlood, Inc. - 2015-11-24](https://www.keypedia.com/records/fda_inspections/oneblood-inc/a97092d5-ec24-492a-ac82-bf817ab38149) — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015
- [FDA Inspection 857474 - OneBlood, Inc. - 2013-12-03](https://www.keypedia.com/records/fda_inspections/oneblood-inc/e7ea7e73-90e9-4f10-8aff-e878c9b88c57) — classification: No Action Indicated (NAI), source: FDA, date: December 3, 2013
- [FDA Inspection 748658 - OneBlood, Inc. - 2011-10-05](https://www.keypedia.com/records/fda_inspections/oneblood-inc/50345c88-7118-4e5a-bbf0-15d36cbf01b0) — classification: No Action Indicated (NAI), source: FDA, date: October 5, 2011
- [FDA Inspection 636513 - OneBlood, Inc. - 2010-01-04](https://www.keypedia.com/records/fda_inspections/oneblood-inc/0bffbed0-6bbd-4aea-ad42-31bb9a511d10) — classification: No Action Indicated (NAI), source: FDA, date: January 4, 2010

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